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丝裂霉素C诱导的大肠杆菌K12类核变化。

Mitomycin-C-induced changes in the nucleoid of Escherichia coli K12.

作者信息

Lossius I, Krüger P G, Male R, Kleppe K

出版信息

Mutat Res. 1983 Apr;109(1):13-20. doi: 10.1016/0027-5107(83)90090-8.

DOI:10.1016/0027-5107(83)90090-8
PMID:6403848
Abstract

The influence of low concentrations of mitomycin-C on the structure of the envelope-free nucleoid was studied in several strains of Escherichia coli K12. The wild-type strain AB1157 uvr+ rec+ and 3 mitomycin-C-sensitive derivatives carrying mutations in the uvrA, uvrB and recA genes, were used. Treatment of the control strain with mitomycin-C, 0.5 microgram/ml, followed by incubation in drug-free medium resulted in the formation of a transient fast-sedimenting nucleoid with a sedimentation coefficient of 2200 S. A fraction of 25% of the nucleoids had attained the normal sedimentation coefficient of 1570 S 3 h after removal of mitomycin-C. With the uvr- strains, mitomycin-C induced a slow, almost linear increase in the S value of the envelope-free nucleoid. In these cases the S value continued to increase during post-incubation and was 2050 S 3 h after removal of the drug. Post-incubation of recA- cells resulted in loss of supercoiling, decrease in S value of the nucleoid and degradation of DNA. Results obtained with phase-contrast and electron microscopy were in good agreement with the hydrodynamic data.

摘要

在几种大肠杆菌K12菌株中研究了低浓度丝裂霉素C对无包膜类核结构的影响。使用了野生型菌株AB1157 uvr+ rec+以及3种在uvrA、uvrB和recA基因中携带突变的丝裂霉素C敏感衍生物。用0.5微克/毫升的丝裂霉素C处理对照菌株,然后在无药物培养基中孵育,导致形成一种沉降系数为2200 S的瞬时快速沉降类核。在去除丝裂霉素C 3小时后,25%的类核达到了1570 S的正常沉降系数。对于uvr-菌株,丝裂霉素C诱导无包膜类核的S值缓慢且几乎呈线性增加。在这些情况下,S值在孵育后继续增加,在去除药物3小时后为2050 S。recA-细胞的孵育后导致超螺旋丧失、类核S值降低和DNA降解。相差显微镜和电子显微镜获得的结果与流体动力学数据高度一致。

相似文献

1
Mitomycin-C-induced changes in the nucleoid of Escherichia coli K12.丝裂霉素C诱导的大肠杆菌K12类核变化。
Mutat Res. 1983 Apr;109(1):13-20. doi: 10.1016/0027-5107(83)90090-8.
2
Effect of methyl methanesulphonate on the nucleoid structure of Escherichia coli.甲磺酸甲酯对大肠杆菌类核结构的影响。
J Gen Microbiol. 1981 May;124(1):159-71. doi: 10.1099/00221287-124-1-159.
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Survival and induction of recA protein in mitomycin C-treated Escherichia coli rec, lex, or uvr strains.丝裂霉素C处理的大肠杆菌rec、lex或uvr菌株中的recA蛋白诱导及存活情况
J Biol Chem. 1983 Nov 25;258(22):13653-7.
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A loss of uvrA function decreases the induction of the SOS functions recA and umuC by mitomycin C in Escherichia coli.uvrA功能的丧失会降低丝裂霉素C在大肠杆菌中对SOS功能recA和umuC的诱导作用。
Mutat Res. 1985 May;149(3):297-302. doi: 10.1016/0027-5107(85)90144-7.
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Respiration shutoff in Escherichia coli K12 strains is induced by far ultraviolet radiations and by mitomycin C.大肠杆菌K12菌株中的呼吸停止是由远紫外线辐射和丝裂霉素C诱导的。
Mutat Res. 1984 Mar;139(3):107-10. doi: 10.1016/0165-7992(84)90002-2.
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Influence of caffeine on the induction of SOS functions recA and umuC by mitomycin C in Escherichia coli.咖啡因对丝裂霉素C在大肠杆菌中诱导SOS功能recA和umuC的影响。
Microbios. 1990;64(260-261):185-95.
7
[The adaptive response to mitomycin C exposure in the hyper-radioresistant mutant Escherichia coli Gamr444].[超放射抗性突变型大肠杆菌Gamr444中对丝裂霉素C暴露的适应性反应]
Tsitologiia. 1991;33(1):88-96.
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[Genetic control of the protective effect of spermidine in Escherichia coli cells as affected by mitomycin C].[亚精胺对丝裂霉素C作用下大肠杆菌细胞保护效应的遗传控制]
Genetika. 1983 Jun;19(6):888-96.
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The sir locus of Escherichia coli: a gene involved in SOS-independent repair of mitomycin C-induced DNA damage.大肠杆菌的sir基因座:一个参与丝裂霉素C诱导的DNA损伤的非SOS依赖修复的基因。
Mutat Res. 1990 Mar;235(2):85-92. doi: 10.1016/0921-8777(90)90061-9.
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Changes in ATP concentration in Escherichia coli during induction of the SOS system by mitomycin C and bleomycin.丝裂霉素C和博来霉素诱导大肠杆菌SOS系统期间ATP浓度的变化
J Gen Microbiol. 1984 Sep;130(9):2247-51. doi: 10.1099/00221287-130-9-2247.

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Effects of quinolones on nucleoid segregation in Escherichia coli.
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